BEUDAMED
    3 results · 26ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    DENALI FEMORAL SYSTEM

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·April 18, 2014

    DA+ C SERIES SR

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code NVZ·October 31, 2012

    PLM A+3 MEDNET WRLSS

    FDA Adverse Event
    Malfunction ·HOSPIRA, INC.·Product code FRN·August 17, 2010